A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055049



Internal ID18797580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46989208..47249575hg19UCSC Ensembl
Innerchr10:46409214..46669581hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19260368
hg18260368
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv765n100
Supporting Variantsnssv3705758
Samples
Known GenesAGAP9, ANXA8, BMS1P2, BMS1P6, FAM25C, FAM25G, GPRIN2, HNRNPA1P33, LINC00842, LOC100996758, NPY4R
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055049
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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